ame-miR-14在意大利蜜蜂工蜂幼虫肠道发育过程的调控作用

【目的】本研究旨在揭示ame-miR-14在意大利蜜蜂Apis mellifera ligustica工蜂幼虫肠道发育过程的调控作用。【方法】通过Stem-loop RT-PCR和Sanger测序分别验证ame-miR-14在意大利蜜蜂工蜂6日龄幼虫肠道中的表达和序列真实性。饲喂ame-miR-14的模拟物(mimic-ame-miR-14)和抑制物(inhibitor-ame-miR-14)及其相应的阴性对照mimic-NC和inhibitor-NC对ame-miR-14分别进行过表达和敲降，利用RT-qPCR检测意大利蜜蜂工蜂4-6日龄幼虫肠道中ame-miR-14的表达量。利用生物信息学软件预测ame-miR-14的靶基因并进行相关分析。利用RT-qPCR检测ame-miR-14的过表达和敲降后其靶基因FoxO和Hedgehog在4-6日龄幼虫肠道中的相对表达量。【结果】ame-miR-14在意大利蜜蜂工蜂6日龄幼虫肠道中真实存在和表达。相较于饲喂mimic-NC,饲喂mimic-ame-miR-14后ame-miR-14表达量在意大利蜜蜂工蜂4-6日龄幼虫肠道中均为显著上调；相...

Regulatory role of ame-miR-14 in the developmental process of the larval guts ofApis mellifera ligustica(Hymenoptera: Apidae) workers

【Aim】 The objective of this study is to unravel the regulatory role of ame-miR-14 in the developmental process of the larval guts of Apis mellifera ligustica workers.【Methods】 The expression and sequence authenticity of ame-miR-14 in the 6-day-old larval guts of A. m. ligustica workers were proved by Stem-loop RT-PCR and Sanger sequencing, respectively. Overexpression and knockdown of ame-miR-14 were conducted by feeding its corresponding mimic (mimic-ame-miR-14) and inhibitor (inhibitor-ame-miR-14), and their corresponding negative controls mimic-NC and inhibitor-NC, respectively, and then RT-qPCR was used to detect the expression levels of ame-miR-14 in the 4-6-day-old larval guts of A. m. ligustica workers. Bioinformatic software was used to predict and analyze the target genes of ame-miR-14. RT-qPCR was employed to detect the relative expression levels of the target genes FoxO and Hedgehog in the 4-6-day-old larval guts after overexpression and knockdown of ame-miR-14.【Results】 ame-miR-14 truly exists and is expressed in the 6-day-old larval guts of A. m. ligustica workers. The expression levels of ame-miR-14 in the 4-6-day-old larval guts of A. m. ligustica workers fed with mimic-ame-miR-14 were significantly up-regulated as compared to those fed with mimic-NC. The expression levels of ame-miR-14 in the 4-6-day-old larval guts of A. m. ligustica workers fed with inhibitor-ame-miR-14 were significantly down-regulated as compared to those fed with inhibitor-NC. In total, ame-miR-14 can target 309 genes, which could be annotated to 45 KEGG pathways and 36 GO terms. Further analysis showed that ame-miR-14 can target 14 genes associated with growth and development and have potential targeting relationship with target genes FoxO and Hedgehog. After overexpression of ame-miR-14, the expression level of FoxO in the 4 day old larval gut of the mimic-ame-miR-14 group was down-regulated and those in the 5- and 6-day-old larval guts significantly down-regulated as compared to those in the mimic-NC group. After knockdown of ame-miR-14, the expression level of FoxO in the 4-day-old larval gut of the inhibitor-ame-miR-14 group was down-regulated, while that in the 5-day-old larval gut was significantly up-regulated and that in the 6-day-old larval gut was up-regulated as compared to those in the inhibitor-NC group. After overexpression of ame-miR-14, the expression levels of Hedgehog in the 4-6-day-old larval guts of the mimic-ame-miR-14 group were significantly down-regulated in comparison with those in the mimic-NC group, whereas those in the 4-6-day-old larval guts of the inhibitor-ame-miR-14 group were up-regulated in comparison with those in the inhibitor-NC group. 【Conclusion】ame-miR-14 truly exists and is expressed in the larval guts of A. m. ligustica workers. Effective overexpression and knockdown of ame-miR-14 in the larval guts of A. m. ligustica workers can be achieved by feeding mimic and inhibitor, respectively. ame-miR-14 potentially participates in regulation of the larval gut development by negatively regulating the expression of FoxO and Hedgehog.